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1 roosting sites in the USA and cultivated on selective media.
2 gene inactivation, which was detected on the selective media.
3 formation of growing cultures and plating on selective media.
4 otic resistance were identified by growth in selective media.
5 es in the host strain, and allowed growth on selective media.
6 defined as good growth on gram-negative rod-selective media.
7 copy and by enumeration on selective and non-selective media.
8 ed in infected mosquito cell clones grown in selective media.
9 . aureus was isolated using nonselective and selective media.
10 s small colonies were noted on Campylobacter selective media after 5 days of microaerobic incubation.
14 samples were enumerated on selective and non-selective media and on doxycycline (4 microg/ml) medium.
15 tly different between colonies directly from selective media and subsequently from pure subculture.
16 ese results were validated by PCR, growth on selective media, and detailed in silico analysis of each
18 ny existing methods, such as plate counts on selective media, automatic (hemocytometer-based) cell co
19 y nasal swabbing proved futile with existing selective media because of extensive overgrowth with Muc
20 occal carriage is culture of throat swabs on selective media, but the levels of carriage determined d
21 lly adapted E. coli strains were isolated on selective media containing ceftriaxone from the wetland
22 ately inoculated on three Bordet Gengou (BG) selective media containing either 0.625 microgram of oxa
23 The aim of this study was to assess five selective media designed for the isolation of Burkholder
26 results, was more sensitive than culture on selective media for samples collected by rectal swab (20
27 ens for culture were obtained, in the use of selective media for Staphylococcus aureus and Haemophilu
28 effective, economical, and readily available selective media for the culture of Clostridium difficile
29 data support the focused use of chromogenic selective media for the increased detection of MRSA in p
30 llowing methods: four types of Campylobacter selective media, four commercial stool antigen assays, a
33 hem with GCV, and then plated the cells into selective media that permitted us to quantify independen
36 cialized laboratory methodology (cultured on selective media, urinary antigen) are applied routinely
37 y, but not all, suspicious colonies grown on selective media within 24 h after inoculation, which sho
38 ecimens, if specimens can be inoculated onto selective media within a relatively short time period no
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